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Catalog Number:
33583
CAS Number:
265321-34-4
Fmoc-4-(acetil-amino)-L-fenilalanina
Purity:
≥ 98 % (HPLC)
Synonym(s):
["["Hasta(1, 1-Dimetiletil)azodicarboxilato, "Bajo la dirección"]
Documents
$65.00 /25 mg
Tamaño
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Product Information

Fmoc-4-(acetyl-amino)-L-phenylalanine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is essential for the selective protection of the amino group during solid-phase peptide synthesis. Its unique structure, characterized by the acetylamino group, enhances its solubility and stability, making it an ideal choice for researchers focused on synthesizing complex peptides and proteins.

In the pharmaceutical industry, Fmoc-4-(acetyl-amino)-L-phenylalanine serves as a building block for the development of peptide-based therapeutics, particularly in the design of inhibitors and biologically active compounds. Its ability to facilitate the incorporation of phenylalanine into peptide chains allows for the exploration of novel therapeutic agents with improved efficacy and specificity. Researchers appreciate its compatibility with various coupling reagents and its ease of deprotection, which streamlines the synthesis process. This compound stands out for its effectiveness in producing high-purity peptides, making it a valuable asset in both academic and industrial laboratories.

Synonyms
["["Hasta(1, 1-Dimetiletil)azodicarboxilato, "Bajo la dirección"]
CAS Number
265321-34-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H24N2O5
Molecular Weight
444.48
MDL Number
MFCD01632242
PubChem ID
53398091
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = -20,8 ± 2 ° (C = 1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
["["Hasta(1, 1-Dimetiletil)azodicarboxilato, "Bajo la dirección"]
CAS Number
265321-34-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C26H24N2O5
Molecular Weight
444.48
MDL Number
MFCD01632242
PubChem ID
53398091
Appearance
Polvo blanco
Optical Rotation
[a] D 25 = -20,8 ± 2 ° (C = 1 en DMF)
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-(acetyl-amino)-L-phenylalanine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a crucial building block in solid-phase peptide synthesis, allowing researchers to create complex peptides efficiently.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in targeting specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The acetyl group facilitates bioconjugation processes, making it valuable in the development of targeted drug delivery systems and imaging agents.
  • Protein Engineering: It is used in modifying proteins to study structure-function relationships, helping researchers understand protein interactions and stability.
  • Research in Cancer Therapy: The compound shows promise in developing peptide therapeutics for cancer treatment, providing a targeted approach with potentially fewer side effects compared to traditional therapies.

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